DeltaV GMP Automation Specialist (CSV/Validation)

Cognizant; Singapore; On-site; SGD 120,000 - 180,000; Full time

Job summary

Cognizant in Singapore seeks an experienced DeltaV Application Programmer to design, configure, and maintain Emerson DeltaV DCS applications within a GMP-regulated pharmaceutical facility.

The role combines batch/continuous software configuration with hardware knowledge in a validated CSV environment, emphasizing documentation, change control, and data integrity for API and biologics operations.

Qualifications

• 10+ years hands-on experience with Emerson DeltaV DCS in GMP settings.
• Strong knowledge of DeltaV software tools and HMI configuration.
• Familiarity with CSV, 21 CFR Part 11 and validation documentation.

Responsibilities

• Design, develop, test, and deploy DeltaV control strategies and S88-based logic.
• Configure DeltaV I/O, alarms, historian tags, and Control Studio displays.
• Maintain DeltaV hardware and network architecture; ensure IT/OT alignment.
• Support IQ/OQ/PQ, FAT/SAT, and change control processes.
• Collaborate with QA, Validation, and Manufacturing teams to ensure compliance.

Skills

DeltaV DCS

GMP/CSV

HMI configuration

Network topology

IQ/OQ/PQ docs

Tools

DeltaV Control Studio

Batch Historian

MES integration

Job description

Cognizant in Singapore seeks an experienced DeltaV Application Programmer to design, configure, and maintain Emerson DeltaV DCS applications within a GMP-regulated pharmaceutical facility.

The role combines batch/continuous software configuration with hardware knowledge in a validated CSV environment, emphasizing documentation, change control, and data integrity for API and biologics operations.